FOAMING HAND SANITIZER- benzalkonium chloride liquid

Foaming Hand Sanitizer by

Drug Labeling and Warnings

Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Specialty Water Resources, Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use

Warnings

For external use only
When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Pump a small amount of foam into palm of hand
Rub thoroughly over all surfaces of both hands
Rub hands together briskly until dry

Inactive Ingredients

Water, d-glucopyranose, oligomeric, decyl octyl glycosides, glycerol, methylisothiazolinone, and citric acid.

SPL UNCLASSIFIED SECTION

For Your Water

"What is your mission?"

no alcohol

dye and fragrance free

soft on skin with moisturizers

MUST BE USED WITH FOAMING DISPENSER / PUMP

MADE IN THE USA

WARNING

KEEP OUT OF REACH OF CHILDREN.

MAY BE HARMFUL IF SWALLOWED.

MAY CAUSE EYE IRRITATION.

SEE BACK PANEL FOR ADDITIONAL PRECAUTIONS AND FIRST AID.

INSTITUTIONAL & COMMERCIAL HAND SANITIZER

Before discarding container, rinse with water.

For institutional and commercial use.

MFG For: For Your Water

11804 Woodruff Ave., Downey, CA 90241

Ph: 1-877-377-9687

For Additional Product and Safety Information
See Safety Data Sheet

Packaging

INGREDIENTS AND APPEARANCE

FOAMING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79724-375
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
2,3 DI-O-METHYL-D-GLUCOSE (UNII: 3F1Y194PDX)
CAPRYL OLIGOGLUCOSIDE (UNII: VXR09E583M)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79724-375-81	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/20/2020

Labeler - Specialty Water Resources, Llc (080769471)